Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCAGGAGAGGGGCACCATCTCAAGT[C/T]GAAGAGACCCAACCCCTGTGCCTAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604399 MIM: 607048 | ||||||||||||||||||||
Literature Links: |
PPP1R1B PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
PPP1R1B - protein phosphatase 1 regulatory inhibitor subunit 1B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001242464.1 | 1017 | Missense Mutation | TCG,TTG | S,L 30 | NP_001229393.1 | |
NM_032192.3 | 1017 | Missense Mutation | TCG,TTG | S,L 66 | NP_115568.2 | |
NM_181505.3 | 1017 | Missense Mutation | TCG,TTG | S,L 30 | NP_852606.1 | |
XM_017025216.1 | 1017 | Missense Mutation | TCG,TTG | S,L 66 | XP_016880705.1 | |
XM_017025217.1 | 1017 | Missense Mutation | TCG,TTG | S,L 30 | XP_016880706.1 |
STARD3 - StAR related lipid transfer domain containing 3 | ||||||
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There are no transcripts associated with this gene. |